Biology subjects

Garrido, L.

Publications and source records attributed to Garrido, L..

6 recordsLinked to original sources

bioRxiv2025

Overlooked neuroanatomical markers of face processing and developmental prosopagnosia in posteromedial cortex

Recent functional imaging studies implicate human posteromedial cortex (PMC)--composed of the posterior cingulate cortex, the precuneus, and retrosplenial cortex--in face processing. Separately, anatomical studies have identified previously overlooked cortical folds (sulci) in PMC associated with higher-level cognitive abilities. Here, we tested whether these newly identified sulci support face processing in neurotypical individuals and individuals with developmental prosopagnosia (DP). After manually labeling 1,642 sulci in 164 hemispheres, we first identified a gradient of face selectivity along the anterior-posterior axis of PMC that was consistent across three samples, including DP individuals. Second, we discovered a new anatomical locus in PMC that differed structurally and functionally between neurotypical and DP individuals. Finally, data-driven analysis revealed that right-hemisphere PMC sulcal morphology was associated with face recognition ability. These findings reveal a sulcal network in PMC that supports face processing, and they identify the first structural neuroanatomical marker of face processing deficits in PMC.

neuroscience↗

bioRxiv2024

Characterization of a marine bacteria through a novel metabologenomics approach

Exploiting microbial natural products is a key pursuit of the bioactive compound discovery field. Recent advances in modern analytical techniques have increased the volume of microbial genomes and their encoded biosynthetic products measured by mass spectrometry-based metabolomics. However, connecting multi-omics data to uncover metabolic processes of interest is still challenging. This results in a large portion of genes and metabolites remaining unannotated. Further exacerbating the annotation challenge, databases and tools for annotation and omics integration are scattered, requiring complex computations to annotate and integrate omics datasets. Here we performed a two-way integrative analysis combining genomics and metabolomics data to describe a new approach to characterize the marine bacterial isolate BRA006 and to explore its biosynthetic gene cluster (BGC) content as well as the bioactive compounds detected by metabolomics. We described BRA006 genomic content and structure by comparing Illumina and Oxford Nanopore MinION sequencing approaches. Digital DNA:DNA hybridization (dDDH) taxonomically assigned BRA006 as a potential new species of the Micromonospora genus. Starting from LC-ESI(+)-HRMS/MS data, and mapping the annotated enzymes and metabolites belonging to the same pathways, our integrative analysis allowed us to correlate the compound Brevianamide F to a new BGC, previously assigned to other function.

biochemistry↗

bioRxiv2022

Hominoid-specific sulcal variability is related to face perception ability

Human perception requires complex cortical networks that function at neuroanatomical scales of microns and temporal scales of milliseconds. Despite this complexity, what if just one morphological feature of the brain could predict perceptual ability? Here, we tested this hypothesis with pre-registered analyses of neuroanatomy and face perception in neurotypical controls (NTs) and individuals with developmental prosopagnosia (DPs). Results show that the length of the mid-fusiform sulcus (MFS), a hominoid-specific tertiary sulcus in ventral temporal cortex (VTC), was shorter in DPs than NTs. Furthermore, individual differences in MFS length in the right, but not left, hemisphere predicted individual differences in face perception. These results support theories linking brain structure and function to perception, as well as indicate that one feature - variability in MFS length - can predict face perception. Finally, these findings add to growing evidence supporting a role of morphological variability of late developing, tertiary sulci and individual differences in cognition.

neuroscience↗

bioRxiv2020

FFA and OFA encode distinct types of face identity information

Faces of different people elicit distinct functional MRI (fMRI) patterns in several face-selective brain regions. Here we used representational similarity analysis to investigate what type of identity-distinguishing information is encoded in three face-selective regions: fusiform face area (FFA), occipital face area (OFA), and posterior superior temporal sulcus (pSTS). We used fMRI to measure brain activity patterns elicited by naturalistic videos of famous face identities, and compared their representational distances in each region with models of the differences between identities. Models included low-level to high-level image-computable properties and complex human-rated properties. We found that the FFA representation reflected perceived face similarity, social traits, and gender, and was well accounted for by the OpenFace model (deep neural network, trained to cluster faces by identity). The OFA encoded low-level image-based properties (pixel-wise and Gabor-jet dissimilarities). Our results suggest that, although FFA and OFA can both discriminate between identities, the FFA representation is further removed from the image, encoding higher-level perceptual and social face information.

neuroscience↗

bioRxiv2019

Age-linked heterogeneity among oligodendrocyte precursor cells in the cerebral cortex of mice and human

Oligodendrocyte precursor cells (OPCs) are responsible for spontaneous remyelination after a demyelinating lesion. They are present in large parts of the mouse and human central nervous system, both during development and in adulthood, yet how their physiological behaviour is modified throughout life remains largely unknown. Moreover, the activity of adult human OPCs is still not fully understood. Significantly, most of the molecules involved in OPC-mediated remyelination are also involved in their development, a phenomenon that may be clinically relevant. In this article, we have systematically analyzed the intrinsic properties of OPCs isolated from the cerebral cortex of neonatal, postnatal and adult mice, as well as those recovered from neurosurgical adult human cerebral cortex tissue. We also analyze the response of these cells to two molecules that have known effects on OPC biology during development and that are overexpressed in individuals with Multiple Sclerosis (MS): FGF2 and anosmin-1. By analyzing intact OPCs for the first time with H-1 HR-MAS NMR spectroscopy, we show that these cells behave distinctly and that they have different metabolic patterns in function of their stage of maturity. Moreover, their response to FGF-2 and anosmin-1 differs in relation to their developmental stage and in function of the species. Our data reveal that the behaviour of adult human and mouse OPCs differs in a very dynamic way that should be considered when testing drugs and for the proper design of effective pharmacological and/or cell therapies for MS.

neuroscience↗

bioRxiv2018

Faces and voices in the brain: a modality-general person-identity representation in superior temporal sulcus

Face-selective and voice-selective brain regions have been shown to represent face-identity and voice-identity, respectively. Here we investigated whether there are modality-general person-identity representations in the brain that can be driven by either a face or a voice, and that invariantly represent naturalistically varying face and voice tokens of the same identity. According to two distinct models, such representations could exist either in multimodal brain regions (Campanella and Belin, 2007) or in face-selective brain regions via direct coupling between face- and voice-selective regions (von Kriegstein et al., 2005). To test the predictions of these two models, we used fMRI to measure brain activity patterns elicited by the faces and voices of familiar people in multimodal, face-selective and voice-selective brain regions. We used representational similarity analysis (RSA) to compare the representational geometries of face- and voice-elicited person-identities, and to investigate the degree to which pattern discriminants for pairs of identities generalise from one modality to the other. We found no matching geometries for faces and voices in any brain regions. However, we showed crossmodal generalisation of the pattern discriminants in the multimodal right posterior superior temporal sulcus (rpSTS), suggesting a modality-general person-identity representation in this region. Importantly, the rpSTS showed invariant representations of face- and voice-identities, in that discriminants were trained and tested on independent face videos (different viewpoint, lighting, background) and voice recordings (different vocalizations). Our findings support the Multimodal Processing Model, which proposes that face and voice information is integrated in multimodal brain regions.\n\nSignificance statementIt is possible to identify a familiar person either by looking at their face or by listening to their voice. Using fMRI and representational similarity analysis (RSA) we show that the right posterior superior sulcus (rpSTS), a multimodal brain region that responds to both faces and voices, contains representations that can distinguish between familiar people independently of whether we are looking at their face or listening to their voice. Crucially, these representations generalised across different particular face videos and voice recordings. Our findings suggest that identity information from visual and auditory processing systems is combined and integrated in the multimodal rpSTS region.

neuroscience↗